EP0217696B1 - Diffusion einer aktiven Verbindung durch Verbrennung von Papier und Verwendung eines solchen Papiers in einem pyrotechnischen Diffusor - Google Patents

Diffusion einer aktiven Verbindung durch Verbrennung von Papier und Verwendung eines solchen Papiers in einem pyrotechnischen Diffusor Download PDF

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Publication number
EP0217696B1
EP0217696B1 EP86401859A EP86401859A EP0217696B1 EP 0217696 B1 EP0217696 B1 EP 0217696B1 EP 86401859 A EP86401859 A EP 86401859A EP 86401859 A EP86401859 A EP 86401859A EP 0217696 B1 EP0217696 B1 EP 0217696B1
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Prior art keywords
nitrocellulose
paper
element according
distributing element
active compound
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EP86401859A
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English (en)
French (fr)
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EP0217696A1 (de
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Patrick Barruet
Alain Fauconnier
Pierre-Régis Carle
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Societe Nationale des Poudres et Explosifs
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Societe Nationale des Poudres et Explosifs
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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01M—CATCHING, TRAPPING OR SCARING OF ANIMALS; APPARATUS FOR THE DESTRUCTION OF NOXIOUS ANIMALS OR NOXIOUS PLANTS
    • A01M1/00—Stationary means for catching or killing insects
    • A01M1/20—Poisoning, narcotising, or burning insects
    • A01M1/2022—Poisoning or narcotising insects by vaporising an insecticide
    • A01M1/2061—Poisoning or narcotising insects by vaporising an insecticide using a heat source
    • A01M1/2066—Poisoning or narcotising insects by vaporising an insecticide using a heat source burning insecticide, e.g. impregnated candles, burning coils
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/20—Combustible or heat-generating compositions
    • C—CHEMISTRY; METALLURGY
    • C06—EXPLOSIVES; MATCHES
    • C06D—MEANS FOR GENERATING SMOKE OR MIST; GAS-ATTACK COMPOSITIONS; GENERATION OF GAS FOR BLASTING OR PROPULSION (CHEMICAL PART)
    • C06D3/00—Generation of smoke or mist (chemical part)

Definitions

  • the invention also relates to fumigation devices, and more particularly pyrotechnic diffusers which use active compounds secured to a combustible support.
  • patent BE 655 516 ensures the diffusion of a chlorinated quinone by combustion of a support constituted either by a mixture of nitrocellulose and melamine or by a filter paper containing nitrate of potassium.
  • the first orientation consisted in seeking a slow and incomplete combustion which corresponds to a consumption occurring at a lower temperature, but often producing dirty and even irritating fumes.
  • the second orientation which is currently the most used, consists in only heating the support of the active compound until reaching the evaporation temperature of this compound.
  • Belgian patent 644,414 which dates from 1964, mentions a consumable body for combating insects whose combustible support is an organic or mineral material, such as kaolin, silica, pumice, limestone, cardboard, paper, wood, wool or cellulose, which is impregnated with an inorganic oxidant such as potassium, barium or lead nitrate or with chlorates, and which includes combustion moderators such as thiourea.
  • an organic or mineral material such as kaolin, silica, pumice, limestone, cardboard, paper, wood, wool or cellulose, which is impregnated with an inorganic oxidant such as potassium, barium or lead nitrate or with chlorates, and which includes combustion moderators such as thiourea.
  • compositions of a pyrotechnic nature, are also used to diffuse much more quickly either pesticides or opacifiers (smoke curtain) or physiological agents (tear gas), but these compositions due to the higher combustion speed, have a higher combustion temperature and give off more smoke.
  • opacifiers smoke curtain
  • physiological agents physiological agents
  • One such example of composition is mentioned in patent FR 2 456 934 which was filed in 1979 by SNPE and which relates to a tear gas canister whose combustible support consists of a polymer, a mineral oxidant and additives allowing combustion regular.
  • Patent FR 2 378 448 filed in 1978 describes one of the methods for combating harmful insects which consists in heating a molded element of porous mineral material impregnated with an active compound, using an ascending current of hot air capable of heat this element to around 200 ⁇ 430 ° C to thus vaporize the active compound in a short time.
  • This patent refers to a prior technique for combating harmful insects which consists in burning the combustible support (incineration method) on which the active compound is secured, and it is indicated that to improve this technique it is necessary to use a large amount of active compound, but despite this, because the active compound is diffused in a state where it adheres to particles of combustion products having a large dimension, it does not obtain sufficient contact of the ingredient active with insects and the effect obtained is weak, these combustion products in the form of smoke can moreover incorrectly trigger the detectors smoke placed in buildings.
  • the patent FR 1 602 618 filed in 1975 and the patent FR 2 0382 192 filed in 1978 describe another method of combating harmful insects which also consists in heating a mixture of an active compound and of a propagating agent indirectly with means of a heating element for thermally decomposing the propagation agent without causing its combustion and for volatilizing the active compound.
  • the patent FR 2 382 192 includes numerous comparative tests based on the effective fugacity rate of the active compounds, which measures the efficiency of the diffusion process and, while according to this indirect heating process the fugacity rates are between 61, 1% and 86.7%, the comparative tests carried out using a pyrotechnic composition which comprises 30% of nitrocellulose only making it possible to obtain fugacity rates of between 1.7% and 8.6% which show the ineffectiveness of these pyrotechnic compositions for diffusing insecticides in particular from the group of pyrethroids.
  • the object of the present invention is to ensure efficient and rapid dispersion by means of a large volume of combustion gases comprising very little smoke and originating from a particular combustion reaction at a limited temperature so as not to degrade the compound.
  • active and the invention is characterized in that on the one hand the paper is a nitrocellulose paper whose nitrogen content is greater than 5%, and in that on the other by the active compound has a higher degradation temperature at 130 ° C.
  • nitrocellulose paper is constituted by a mixture of binding fibers and nitrocellulose fibers, this mixture comprising at least 18% of binding fibers, at least half of which are cellulose fibers.
  • This nitrocellulose paper has a density of between 0.35 g / cm 3 and 1.3 g / cm 3 , the densities of less than 0.70 g / cm 3 being more efficient both from the point of view of the possibilities of fixing the active compound only from the point of view of combustibility at moderate temperature, in particular when the thickness of this nitrocellulose paper is between 0.2 millimeter and 2.5 millimeters.
  • the nitrocellulose papers can also contain a resin, but when the active compound to be dissipated is a pesticide, it is then very desirable that the resin content of the nitrocellulose paper is less than 2% because the resins used in the paper industries, and which are often polymers, increase the volume of the fumes emitted and give these fumes an unpleasant pungent odor.
  • the active compound to be dissipated is a physiological agent such as a tear gas agent used by the police, there is no disadvantage in using resin levels of up to 6 or 8%, this much higher rate of resin resulting in the production of more unpleasant fumes but still allowing an exothermic decomposition reaction of the nitrocellulose to be maintained at a limited temperature.
  • nitrocellulose diffusing paper When the nitrocellulose diffusing paper is not used quickly after its manufacture, which is the general case, it is then essential that this paper comprises a nitrocellulose stabilizer, a rate of 0.5 to 1.5% of stabilizer being sufficient.
  • nitrocellulose which is used in pyrotechnics for these explosion-proof properties (gun powder) and its properties of lively combustion generating gas (propellants), could in intimate combination with cellulose fibers decompose thermally at a relatively low temperature of 130 ° C and 350 ° C, provided however that the reaction is initiated by appropriate ignition and is carried out at atmospheric pressure.
  • the active compound is distributed in the mass of the nitrocellulose paper by impregnation in the liquid phase, the best results being obtained with a liquid phase produced from a liquid base which is not a gelatinizing solvent for nitrocellulose,
  • a liquid base which is not a gelatinizing solvent for nitrocellulose
  • the particular choice of this liquid base depends on the nature of the active compound and it is preferable that this compound is soluble in the liquid impregnation base, the main bases to be avoided because of their gelatinizing action of nitrocellulose being: ether, acetone, tetrahydrofuran, dimethylformamide and cyclohexanone.
  • the liquid impregnation base can in particular be chosen from the group consisting of: alcohols, methylene chloride, dimethylsulfoxide, hexamethylphosphotriamide, benzene, toluene and xylene.
  • the nitrocellulose paper impregnated with active compound can be burnt in the open air, but both for reasons of convenience of safety of use and transport, and for reasons of efficiency of diffusion, it is preferable that this paper is placed in a pyrotechnic diffuser which is presented as a small box provided with openings, equipped with an ignition device. Under such conditions of use, the work relating to this invention has demonstrated that the maximum temperature reached at the center of the diffuser cannot be lowered below 200 ° C. and under these conditions of use, in order to obtain good diffusion of the active compound in the combustion gases, it is then necessary for the degradation temperature of this compound to be greater than 170 ° C.
  • the invention is more particularly adapted to the diffusion of active compounds which comprise one or more pesticides, and in particular insecticides or insect repellents, and the invention has made it possible to obtain remarkable results for ensuring the diffusion of insecticides belonging to the group of pyrethroids or assimilated to persistence of action, and in particular: deltamethrin, tralomethrin, cypermethrin, permethrin, cyfluthrin, cyhalothrin, fenfluthrin, fencythrine and fenvalerate.
  • the ratio between the length and the width of the strip is between 3 and 10, this strip comprising undulations or folds so as to reduce the contact zones with the bottom of the diffuser, which allows on the one hand to reduce the heating of the wall of the diffuser and on the other hand to approach the conditions of exothermic decomposition in the open air by avoiding any confinement due to the walls of the box.
  • Another advantage which if it is not an imperative operating condition is nonetheless very interesting, is the considerable reduction of the fumes emitted despite the rapid diffusion of the active compounds, since for example it is possible in 10 seconds to treat a room of 50 m 3 ein producing only smoke similar to a puff of cigar.
  • nitrocellulose papers Numerous formulations of nitrocellulose papers have been produced and, for example, the results mentioned in Table 1 have been obtained by preparing nitrocellulosic pulp on the one hand with shredded kraft paper as a source of cellulose fibers, and on the other hand with nitrocellulose, the nitrogen level of which is 13.48, the stabilizer used being diphenylamine and the flocculation resin (acrylic emulsion) being introduced at a variable rate.
  • nitrocellulose paper itself has no insecticidal effect.
  • the irritant effect of the combustion gases does not present any disadvantage during the diffusion of physiological agents such as tear gas, and on the contrary reinforces the effectiveness of action of these physiological agents.
  • Table 2 shows that it is deltamethrin which presents the greatest variation in the percentage of insecticide remaining active when the temperature varies between 250 ° C and 330 ° C and it is therefore with this insecticide from the group of photostable pyrethroids that biological tests are the most sensitive and the most convincing, this sensitivity beyond 270 ° C explaining some deviations observed during the experiments.
  • thermodegradation of deltamethrin was therefore carried out in order to obtain additional data making it possible to interpret the efficacy tests on different insects, and the results of this study are shown in Table 3.
  • this insecticide was dissolved in methylene chloride, which is not a gelatinizing solvent for nitrocellulose, and this liquid impregnation phase was prepared by dissolving from 0.1 to 0 , 2 g of deltamethrin per cubic centimeter of methylene chloride, this dose of 100 to 200 milligrams of deltamethrin can be directly absorbed in the mass by an amount of nitrocellulose paper between 0.75 g and 2 g.
  • the study under the electron microscope shows that deltamethrin preferentially crystallizes on cellulose fibers and the photographs show the excellent adhesiveness of deltamethrin on all fibers, the microcrystals coating these fibers and in particular those of nitrocellulose.
  • the microcrystals are more numerous in the vicinity of the faces of the nitrocellulose paper but the distribution in the mass is fairly homogeneous when the thickness of the paper is less than one millimeter, the homogenization can be improved by slowing down the evaporation of methylene chloride, which normally evaporates in the open air, after 5 to 10 minutes of exposure.
  • the comparative diffusion tests for active compounds were carried out using the pyrotechnic diffuser shown in FIG. 1 in axial longitudinal section.
  • the active part of the diffuser consists of a metal box (1) which is provided with a central ignition device (2) and which contains at least one element of diffusing paper (3), a removable cover (4) in plastic material ensuring sealing during storage and transport.
  • the metal box comprises a bottom (5) crimped on the cylindrical shell (6), and after filling of this sub-assembly the diffusion cover (7) is also crimped on the top of the cylindrical shell.
  • This diffusion cover comprises two diametrically opposite circular vents (7a), and a pyrotechnic match (2) which is fixed in the center, the friction initiation composition (8) being external to the box.
  • This pyrotechnic match comprises a pyrotechnic delay (9) of 5 seconds and a relay charge (10) constituted by a wick impregnated with black powder.
  • the diffusing paper loads that have been tested are 0.5 g-1 g-2 g and 4 g of nitrocellulose paper, impregnated with deltamethrin at the rate of 50 mg-100 mg and 200 mg per gram of nitrocellulosic paper.
  • the diffusing paper elements (3) are rectangular and placed in bulk inside the box.
  • the heat flux generated by the ignition device initiates the exothermic decomposition reaction of nitrocellulose, which is accompanied by a strong evolution of gases, and these gases, accompanied by a little smoke mainly coming from the combustion of fibers. bond, entrain the active compound through vents and rapidly diffuse in the entire enclosed volume in which the pyrotechnic diffuser is placed.
  • test results given below correspond to the use of a pyrotechnic diffuser, the metal box of which has a diameter of 45 millimeters and a height of 62 millimeters, the diameters of two vents being 10 millimeters.
  • the temperature measurements carried out with a thermocouple show the weak heating of the metal box, the maximum temperatures reached being essentially a function of the nitrocellulose rate of the nitrocellulose paper, of the mass of paper placed in the diffuser box and the type of igniter used.
  • Biological indicators included adults of Musca domestica (Md) caterpillars (L4) of Spodoptera littoralis (SI), adults of Acanthoscelides obtectus (Ao Bruchid beetles) and adults of Aphis craccivora (Ac Aphid).
  • the nitrocellulose paper used was also 65% nitrocellulose (13.8% N2) and the impregnation of deltamethrin (M) being 0.1 or 0.2 g per gram of paper. The results obtained are recorded in Table 5, each value indicated being the average of the two or three tests carried out under each of the conditions tested.
  • the diffusers with the numbers 2, 3 or 5 were regularly distributed along the greenhouse and ignited simultaneously.
  • the closing times of greenhouses for treatment are commonly 8 hours to 12 hours, and the rate of abatement after 1 hour is therefore only a very interesting indication of efficiency which does not, however, correspond to the actual rate of 'reduction (with the exception of the rates of 100%) can be obtained with normal closing times and a weak wind, a zero wind is not desirable especially when the diffusers are very far from each other.
  • the complete destruction of the caterpillars of Spodoptera littoralis was obtained within 3 h 30 to 5 h in the same plastic greenhouse on days of light wind and zero wind, by arranging 3 diffusers each containing 4 grams of paper nitrocellulosics impregnated at 0.05 g of deltamethrin per gram of paper.
  • the reduction rate of Whiteflies (Hemiptera) in greenhouses of the plastic tunnel type currently remains less good, but the only tests carried out were with diffusers whose fugacity rate was only 45%.
  • Other tests carried out in the closed laboratory room made it possible to reach abatement rates of 80% and even 98% after a contact time of 4 hours to 15 hours.

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  • Life Sciences & Earth Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Plant Pathology (AREA)
  • Toxicology (AREA)
  • Chemical & Material Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Dentistry (AREA)
  • Agronomy & Crop Science (AREA)
  • Botany (AREA)
  • Insects & Arthropods (AREA)
  • Combustion & Propulsion (AREA)
  • Organic Chemistry (AREA)
  • Paper (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Air Bags (AREA)
  • Fats And Perfumes (AREA)
  • Diaphragms For Electromechanical Transducers (AREA)
  • Making Paper Articles (AREA)
  • Compounds Of Unknown Constitution (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Claims (22)

  1. " 1. Element zur Wirkstoffverteilung, bestehend aus einem brennbaren Träger und mindestens einem Wirkstoff wie einem Pesticid oder einem tränenreizenden Mittel, dadurch gekennzeichnet, daß der brennbare Träger ein Nitrocellulosepapier ist, das 50 bis 75% Nitrocellulosefasern und mindestens 18% Verbindungsfasern enthält, von denen mindestens die Hälfte Cellulosefasern sind, wobei der Stickstoffgehalt des Papiers über 5% beträgt, und der Wirkstoff eine Zersetzungstemperatur oberhalb 130°C besitzt.
  2. 2. Element zur Wirkstoffverteilung nach Anspruch 1, dadurch gekennzeichnet, daß das Nitrocellulosepapier eine Dichte von 0,35 bis 1,3 g/cm3 aufweist.
  3. 3. Element zur Wirkstoffverteilung nach Anspruch 2, dadurch gekennzeichnet, daß die Dicke das Nitrocellulosepapiers 0,2 bis 2,5 mm beträgt.
  4. 4. Element zur Wirkstoffverteilung nach einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, daß das Nitrocellulosepapier ein Stabilisierungsmittel für die Nitrocellulose enthält.
  5. 5. Element zur Wirkstoffverteilung nach einem der Ansprüche 1 bis 4, dadurch gekennzeichnet, daß das Verhältnis des Gewichts des Wirkstoffs zum Gewicht des Nitrocellulosepapiers kleiner als 0,5 ist.
  6. 6. Element zur Wirkstoffverteilung nach einem der Ansprüche 1 bis 5, dadurch gekennzeichnet, daß der Wirkstoff in der Masse des Nitrocellulosepapiers selbst verteilt ist.
  7. 7. Element zur Wirkstoffverteilung nach Anspruch 6, dadurch gekennzeichnet, daß der Wirkstoff durch Imprägnierung in flüssiger Phase in der Masse des Nitrocellulosepapiers verteilt ist.
  8. 8. Element zur Wirkstoffverteilung nach Anspruch 7, dadurch gekennzeichnet, daß die flüssige Phase zur Imprägnierung des Nitrocellulosepapiers aus einer flüssigen Basis hergestellt wird, die kein Lösungsmittel ist, das Nitrocellulose gelatiniert.
  9. 9. Element zur Wirkstoffverteilung nach Anspruch 8, dadurch gekennzeichnet, daß der Wirkstoff in der flüssigen, zur Imprägnierung verwendeten Basis löslich ist.
  10. 10. Element zur Wirkstoffverteilung nach Anspruch 9, dadurch gekennzeichnet, daß die zur Imprägnierung verwendete flüssige Basis unter Alkoholen, Methylenchlorid, Dimethylsulfoxid, Hexamethylphosphortriamid, Benzol, Toluol und Xylol ausgewählt ist.
  11. 11. Element zur Wirkstoffverbindung nach einem der Ansprüche 1 bis 10, dadurch gekennzeichnet, daß der Wirkstoff eine Zersetzungstemperatur oberhalb 170°C aufweist.
  12. 12. Element zur Wirkstoffverteilung nach einem der Ansprüche 1 bis 11, dadurch gekennzeichnet, daß der Wirkstoff ein oder mehrere Pesticide umfaßt.
  13. 13. Element zur Wirkstoffverteilung nach Anspruch 12, dadurch gekennzeichnet, daß die Pesticide Insecticide oder Insectifuge sind.
  14. 14. Element zur Wirkstoffverteilung nach Anspruch 13, dadurch gekennzeichnet, daß die Insecticide zur Gruppe der Pyrethrinoide oder vergleichbarer Verbindungen mit Wirkungspersistenz gehören.
  15. 15. Element zur Wirkstoffverteilung nach Anspruch 14, dadurch gekennzeichnet, daß das Pyrethrinoid oder die vergleichbare Verbindung unter Deltamethrin, Tralomethrin, Cypermethrin, Permethrin, Cyfluthrine, Cyhalothrine, Fenfluthrine, Fencythrine und Fenvalerat ausgewählt ist.
  16. 16. Element zur Wirkstoffverteilung nach Anspruch 14, dadurch gekennzeichnet, daß das Verhältnis des Gewichts des Pyrethrinoids zum Gewicht des Nitrocellulosepapiers im Bereich von 0,05 bsi 0,25 liegt.
  17. 17. Element zur Wirkstoffverteilung nach einem der Ansprüche 1 bis 16, dadurch gekennzeichnet, daß das Nitrocellulosepapier ferner ein engebrachtes Harz in einer Menge unter 2% aufweist.
  18. 18. Element zur Wirkstoffverteilung nach einem der Ansprüche 1 bis 17, dadurch gekennzeichnet, daß es in Bandform vorliegt.
  19. 19. Pyrotechnischer Diffusor, der eine Dose (1) umfaßt, die mit Gasabzugsöffnungen (7a) sowie einer Zündeinrichtung (2) versehen ist und einen Brennstoff (3) enthält, der die Verteilung eines Wirkstoffs gewährleistet, dadurch gekennzeichnet, daß der Brennstoff ein Element zur Wirkstoffverteilung nach einem 'der Ansprüche 1 bis 18 ist.
  20. 20. Pyrotechnischer Diffusor nach Anspruch 19, dadurch gekennzeichnet, daß das Verhältnis der Gesamtfläche der Gasabzugsöffnungen (7a) und der Masse des Nitrocellulosepapiers 0,3 bis 7 beträgt.
  21. 21. Pyrotechnischer Diffusor nach Anspruch 19, dadurch gekennzeichnet, daß das Verhältnis der Gesamtfläche der Gasabzugsöffnungen zum Innenvolumen der Dose (1) 0,008 bis 0,05 beträgt.
  22. 22. Pyrotechnischer Diffusor nach Anspruch 19, dadurch gekennzeichnet, daß das Verhältnis der Masse des Nitrocellulosepapiers zum Innenvolumen der Dose (1) 0,005 bis 0,2 beträgt.
EP86401859A 1985-08-27 1986-08-22 Diffusion einer aktiven Verbindung durch Verbrennung von Papier und Verwendung eines solchen Papiers in einem pyrotechnischen Diffusor Expired - Lifetime EP0217696B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR8512753 1985-08-27
FR8512753A FR2586673A1 (fr) 1985-08-27 1985-08-27 Papier diffusant un compose actif par combustion et diffuseur pyrotechnique utilisant un tel papier

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EP0217696A1 EP0217696A1 (de) 1987-04-08
EP0217696B1 true EP0217696B1 (de) 1990-08-08

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US (2) US4777032A (de)
EP (1) EP0217696B1 (de)
JP (1) JPS6253499A (de)
AT (1) ATE55213T1 (de)
AU (1) AU584451B2 (de)
BR (1) BR8604069A (de)
DE (1) DE3673304D1 (de)
DK (1) DK405186A (de)
ES (1) ES2000291A6 (de)
FR (1) FR2586673A1 (de)
GR (1) GR862196B (de)
HU (1) HUT58179A (de)
IN (1) IN164778B (de)
PL (1) PL261195A1 (de)
RO (1) RO95763B (de)

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DE10329496A1 (de) * 2003-06-30 2005-02-17 Siemens Ag Unidirektionale Leuchtvorrichtung zum Beleuchten von Objekten und/oder Markieren von Fahrbahnen, vorzugsweise im Flughafenbereich
KR101404913B1 (ko) 2006-05-25 2014-06-09 다우 아그로사이언시즈 엘엘씨 스피노신 훈증제
UA107101C2 (xx) * 2012-07-04 2014-11-25 Інсектицидна шашка (варіанти)
US20160236858A1 (en) * 2015-02-18 2016-08-18 Olen A. Bielski, Iii Packaging system with sealing lid for a votive candle
WO2019159906A1 (ja) 2018-02-16 2019-08-22 三菱瓦斯化学株式会社 トリシクロ［５．２．１．０２，６］デカン－２－カルボン酸エステルの製造方法

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FR1002108A (fr) * 1946-07-27 1952-03-03 Procédé et appareils pour la destruction de mouches, moustiques et autres insectes
US2551406A (en) * 1949-02-28 1951-05-01 Tobacco By Products And Chemic Fumigating package
IT599574A (de) * 1957-11-18
FR1602618A (en) * 1965-10-30 1971-01-04 Heat-dispersed pesticides - separated from the heat source by heat-conducting film
US3391036A (en) * 1966-12-23 1968-07-02 Defence Uk Riot control charges
US3856933A (en) * 1968-03-04 1974-12-24 Dow Chemical Co Pyrotechnic disseminating system
GB1601095A (en) * 1977-01-31 1981-10-21 Sumitomo Chemical Co Controlling agent for and a method of controlling injurious insects
US4163038A (en) * 1977-03-03 1979-07-31 Earth Chemical Company, Limited Fumigating method and apparatus
JPS53118525A (en) * 1977-03-28 1978-10-17 Fuji Kaseiyaku Kk Production of smoking agent of substance having envading * insecticide * bactericide or contorolling propert0y of harmful organism
US4199548A (en) * 1977-06-10 1980-04-22 Toyo Ink Manufacturing Co., Ltd. Thermally diffusible composites
JPS55108278A (en) * 1979-02-08 1980-08-20 Earth Chem Corp Ltd Fumigant and fumigation
FR2500265A1 (fr) * 1981-02-20 1982-08-27 Roussel Uclaf Compositions pesticides contenant un melange synergique de 1r, cis 2,2-dimethyl 3(2,2-dihalovinyl) cyclopropane-1-carboxylate de (s) a-cyano 3-phenoxybenzyle et d'autres composes pyrethrinoides
JPS58131905A (ja) * 1982-01-29 1983-08-06 Yuukou Yakuhin Kogyo Kk 有害生物のくん煙防除剤およびその製造方法

Also Published As

Publication number Publication date
ES2000291A6 (es) 1988-02-01
DE3673304D1 (de) 1990-09-13
RO95763B (ro) 1988-11-01
FR2586673A1 (fr) 1987-03-06
IN164778B (de) 1989-05-27
RO95763A (ro) 1988-10-30
DK405186A (da) 1987-02-28
HUT58179A (en) 1992-02-28
PL261195A1 (en) 1987-05-18
DK405186D0 (da) 1986-08-26
ATE55213T1 (de) 1990-08-15
GR862196B (en) 1986-12-31
US4859454A (en) 1989-08-22
US4777032A (en) 1988-10-11
EP0217696A1 (de) 1987-04-08
AU6159786A (en) 1987-03-05
BR8604069A (pt) 1987-04-07
AU584451B2 (en) 1989-05-25
JPS6253499A (ja) 1987-03-09

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